161 related articles for article (PubMed ID: 12937415)
1. The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease.
Haïk S; Faucheux BA; Sazdovitch V; Privat N; Kemeny JL; Perret-Liaudet A; Hauw JJ
Nat Med; 2003 Sep; 9(9):1121-3. PubMed ID: 12937415
[TBL] [Abstract][Full Text] [Related]
2. Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease.
Favereaux A; Quadrio I; Vital C; Perret-Liaudet A; Anne O; Laplanche JL; Petry KG; Vital A
Arch Neurol; 2004 May; 61(5):747-50. PubMed ID: 15148153
[TBL] [Abstract][Full Text] [Related]
3. Alpha-synuclein-immunoreactive deposits in human and animal prion diseases.
Haïk S; Privat N; Adjou KT; Sazdovitch V; Dormont D; Duyckaerts C; Hauw JJ
Acta Neuropathol; 2002 May; 103(5):516-20. PubMed ID: 11935269
[TBL] [Abstract][Full Text] [Related]
4. [Sporadic Creutzfeldt-Jakob disease: phenotypic variability].
Moreno MJ; Romero J
Neurologia; 2002; 17(7):366-77. PubMed ID: 12236956
[TBL] [Abstract][Full Text] [Related]
5. Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease.
Tabaton M; Monaco S; Cordone MP; Colucci M; Giaccone G; Tagliavini F; Zanusso G
Ann Neurol; 2004 Feb; 55(2):294-6. PubMed ID: 14755736
[TBL] [Abstract][Full Text] [Related]
6. Mechanism of intestinal entry of infectious prion protein in the pathogenesis of variant Creutzfeldt-Jakob disease.
Ghosh S
Adv Drug Deliv Rev; 2004 Apr; 56(6):915-20. PubMed ID: 15063598
[TBL] [Abstract][Full Text] [Related]
7. Emerging pharmacotherapies for Creutzfeldt-Jakob disease.
Korth C; Peters PJ
Arch Neurol; 2006 Apr; 63(4):497-501. PubMed ID: 16606761
[TBL] [Abstract][Full Text] [Related]
8. Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob disease.
Faucheux BA; Privat N; Brandel JP; Sazdovitch V; Laplanche JL; Maurage CA; Hauw JJ; Haïk S
J Neuropathol Exp Neurol; 2009 Aug; 68(8):892-901. PubMed ID: 19606064
[TBL] [Abstract][Full Text] [Related]
9. Pathogenesis and prevalence of variant Creutzfeldt-Jakob disease.
Hilton DA
J Pathol; 2006 Jan; 208(2):134-41. PubMed ID: 16362983
[TBL] [Abstract][Full Text] [Related]
10. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.
Capellari S; Cardone F; Notari S; Schininà ME; Maras B; Sità D; Baruzzi A; Pocchiari M; Parchi P
Neurology; 2005 Mar; 64(5):905-7. PubMed ID: 15753435
[TBL] [Abstract][Full Text] [Related]
11. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.
Schoch G; Seeger H; Bogousslavsky J; Tolnay M; Janzer RC; Aguzzi A; Glatzel M
PLoS Med; 2006 Feb; 3(2):e14. PubMed ID: 16354106
[TBL] [Abstract][Full Text] [Related]
12. BSE and vCJD cause disturbance to uric acid levels.
Lekishvili T; Sassoon J; Thompsett AR; Green A; Ironside JW; Brown DR
Exp Neurol; 2004 Nov; 190(1):233-44. PubMed ID: 15473996
[TBL] [Abstract][Full Text] [Related]
13. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.
Lewis V; Hill AF; Klug GM; Boyd A; Masters CL; Collins SJ
Neurology; 2005 Jul; 65(1):113-8. PubMed ID: 16009895
[TBL] [Abstract][Full Text] [Related]
14. Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle.
Kovacs GG; Lindeck-Pozza E; Chimelli L; Araújo AQ; Gabbai AA; Ströbel T; Glatzel M; Aguzzi A; Budka H
Ann Neurol; 2004 Jan; 55(1):121-5. PubMed ID: 14705121
[TBL] [Abstract][Full Text] [Related]
15. Spatial relationships between diffuse prion protein deposits and neuronal perikarya in variant Creutzfeldt-Jakob disease.
Armstrong RA
Folia Neuropathol; 2013; 51(1):18-25. PubMed ID: 23553133
[TBL] [Abstract][Full Text] [Related]
16. Dilated cardiomyopathy and Creutzfeldt-Jakob disease: evidence for a role of cellular prion protein in the heart?
Bianchin MM; Walz R; Brentani RR; Martins VR
Arch Intern Med; 2005 Jul; 165(14):1663-4. PubMed ID: 16043687
[No Abstract] [Full Text] [Related]
17. [Morphological changes and prion accumulation in the cerebellar cortex in Creutzfeldt-Jacob disease].
Karmysheva VIa; Gulevskaia TS; Pogodina VV
Arkh Patol; 2007; 69(6):10-5. PubMed ID: 18290372
[TBL] [Abstract][Full Text] [Related]
18. Molecular diagnostic tools in Creutzfeldt-Jakob disease and other prion disorders.
Van Everbroeck B; Boons J; De Leenheir E; Lübke U; Cras P
Expert Rev Mol Diagn; 2004 May; 4(3):351-9. PubMed ID: 15137902
[TBL] [Abstract][Full Text] [Related]
19. Serial EEG findings in sporadic and iatrogenic Creutzfeldt-Jakob disease.
Wieser HG; Schwarz U; Blättler T; Bernoulli C; Sitzler M; Stoeck K; Glatzel M
Clin Neurophysiol; 2004 Nov; 115(11):2467-78. PubMed ID: 15465434
[TBL] [Abstract][Full Text] [Related]
20. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
Hoshino A; Iwasaki Y; Izumi M; Kimura S; Ibi T; Kitamoto T; Yoshida M; Hashizume Y; Sahashi K
Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]